General Quality Control Services

December 15, 2019
  • Pharmaceutical waters (PW, WFI, CS) testing
  • Critical systems (N2 distribution, compressed air distribution) testing
  • Environmental monitoring of classified areas (Class A, B, C and D)
  • Raw materials testing and release
  • Primary packaging materials testing and release
  • Secondary packaging materials testing and release
  • Active Pharmaceutical Ingredient (DS) analyses
  • In-Process Control (IPC)
  • Final product (DP) analyses
  • Complete development, qualification and validation of analytical methods to
    comply with international guidelines (ICH, EMA, FDA, etc.).
  • Transfer of analytical methods (<1224> USP)
  • Implementation and verification of Compendial methods (Eur. Ph., USP,
    international Pharmacopoeias)
  • Stability studies according to international guidelines (ICH, WHO, etc.)

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